Pilar Viladas, a bonafide architecture writer and editor, and former AN Best of Design juror, died on March 15 at a ...
The U.S. Food and Drug Administration approved treatment for 11 patients with the rare familial ALS caused by mutations in ...
The first study participant was enrolled in July 2024, and since that time, the consortium has recruited over 300 ...
As Oklahoma lawmakers consider House Bill 1278, which aims to fund research and care for those battling Amyotrophic Lateral Sclerosis (ALS), Michael Wilson and his family share firsthand their ...
Kansas Supreme Court Justice Evelyn Wilson will retire, effective July 4, following a recent amyotrophic lateral sclerosis ...
In one tiny town, more than a dozen people were diagnosed with the rare neurodegenerative disease ALS. Why? I n March 2009, ...
On March 18, 2025, Lila Lou Guazzini took the outreached hand of God and stepped over into a new life. There had to be a crowd waiting for her, as she was a very special lady. Lila was born Feb. 18, ...
It's a list of people who have championed local news and supporting their communities. It's also got more than a couple of familiar voices, like former NHLer Lou Nanne and former "KG Morning Show" ...
Raziel Green, 52, an active runner and mother of two, was diagnosed with a rare form of ALS in 2017. The former retail manager first started experiencing symptoms more than 10 years ago ...
The Atlantic water temperatures have not recovered from the winter chill yet as the heat builds into the 90s over land setting up enhanced velocities to the sea breezes this week. Read full ...
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